L3 - Pathology Terms Flashcards

better understanding of pathology terms and should be able to describe differences between similar entities - read previous lectures on : - Inflammation - Neoplasia - Cell adaptation

1
Q

What is common between a cyst and an abscess

A

Both are cavities which are lined by tissue and condensed fluid

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is a cyst

A

A cavity which is lined by epithelium and filled with condensed fluid or secretions which vary depending on the type of epithelium lining.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

When is the secretion in a cyst watery?

A

When the lining epithelium is serous e.g. The pleura that surrounds the lungs in the pleural cavity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

When is the secretion in a cyst mucusy

A

if the lining epithelium is mucus-secreting columnar epithelium e.g. Goblet cells are found in the respiratory and gastrointestinal tracts

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is an abscess

A

a cavity lined by granulation tissue and pus made from dead or dying neutrophil leukocytes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is a similarity between gruanulation tissue and a granuloma

A

they are both types of tissue that can form as part of the body’s response to injury or inflammation although they are 2 completely different lesions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is granulation tissue

A

(pink tissue that grows over a wound during healing) a repair tissue that consists of newly formed blood vessels, myofibroblasts and immune cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what is the puprose of the newly formed blood vessels and myofibroblasts in granulation tissue

A
  • blood vessels bring in nutrients and oxygen for the repair process (and transport immune cells to fight infection and clear debris)
  • Myofibroblasts bring in the collagen which creates the flexible matrix to support and strengthen the newly formed tissue
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are granulomas

A

a type of chronic inflammation characterised by an accumulation of modified macrophages ( epithelioid histiocytes) and other immune cells. It is a type 4 delayed hypersensitivity reaction and is commonly association with conditions like tuberculosis and sarcoidosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what are epithelioid histiocytes

A

macrophages that have acquired an elongated, eputhelial like shape. They form tight clusters around the foreign substance (or irritant) walling them off to prevent spread.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is the clinical appearance for granulomas

A

hard lumps (e.g. skin or lungs)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the process for granuloma formation caused by persistent TB

A
  • macrophages present antigens via their MHC class II to CD4+ helper t cells
  • Macrophages secrete IL_12 inducing the CD4+ helper cell to differentiate into Th1 subtypes which secrete IFN-y.
  • IFN-y convert macrophages into epitheloid histiocytes and giant cells which get structured around a central core of necrotic cell debris ( where most of the bacteria is concentrated)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Apoptosis vs Necrosis

A
  • Apoptosis is a form of programmed and controlled cell death
  • Necrosis is uncontrolled cell death due to injury or disease
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is apoptosis

A

programmed cell death regulated by intracellular programms in which cells destined to die activate enzymes that degrade the cells’ own DNA and nuclear and cytoplasmic proteins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are the key morphological features of apoptosis

A
  1. Cell shrinkage: The cell volume decreases and there is loss of specialised surface structures.
  2. Chromatin condensation: Nuclear chromatin condenses and aggregates peripherally under the nuclear membrane
  3. Formation of apoptotic bodies: The cell fragments into membrane-bound vesicles containing cellular organelles and nuclear material.
  4. Phagocytosis of apoptotic bodies: Apoptotic bodies are rapidly engulfed and cleared by phagocytes (primarily macrophages) WITHOUT triggering inflammation.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is necrosis

A

the premature death of cells and living tissue caused by factors external to the cells or tissue e.g. infection toxins or trauma. It includes a spectrum of morphologic changes and is largely due to the progressive degradation of enzymes from the cell (lysosomes) or from leukocytes (neutrophils) that are recruited to the site of injury. this process evokes an acute inflammatory reaction and causes major disturbance of surrounding tissue

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

what are example subtypes of necorsis

A
  1. Coagulative necrosis - when blood flow is reduced/ stopped causing the cells to dry and become hard ( and white) e.g. heart, kidney and spleen and occurs
  2. Liquiefactive necrosis - (fat) cells dissolve and turn into a thick sticky liquid e.g. in the brain
  3. Suppurative necrosis - liquefactive necrosis with pus formation
  4. Caseus necrosis
  5. Fat necrosis - enzymatic destruction of fat tissue
  6. Gangrene
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Plasia definition

A

suffix that means formation, growth, or proliferation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What is Hyperplasia

A

an increase in the number of cells in an organ or tissue.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What is neoplasia

A

abnormal and uncontrolled cell growth that is independent of normal regulatory mechanisms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Example of when hyperplasia vs neoplasia may occur

A

Hyperplasia happens in response to physiological demand e.g. Thyroid enlargement during pregnancy to meet increased thyroxine demand, but after pregnancy the thyroid will go back to normal .

Neoplasia happens when there are genetic mutations usually in oncogenes or tumour suppressor genes which result in the uncontrolled proliferation of cells e.g. thyroid tumour which wont regress

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

what controls hyperplasia

A

Hyperplasia is regulated by NEGATIVE FEEDBACK.
(It involves the increase in the number of cells which is under negative feedback control. As soon as the demand is withdrawn, the tissue or organ will go back to its normal size)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

why is neoplastic growth uncontrolled? (why is neoplasia uncontrolled)

A

because it is not regulated by negative feedback. this means that the tissue/ organ doesn’t go back to normal even with the initial stimulus is withdrawal and the cells will continue to grow as genetic control on cell proliferation is lost

24
Q

What is hypertrophy

A

the increase in the SIZE of cells in response to the increase in demand, which therefore increases the size of the organ or tissue.

25
Q

how do cells increase in size in hypertrophy

A

by acquiring more organelles in the cytoplasm

26
Q

Hyperplasia vs hypertrophy

A

Both are in response to increased demand, but hyperplasia is an increase in cell number in cells that are able to multiply (liable cells e.g. epithelial cells of the gut), while hypertrophy is an increase in cell size in cells that are unable to multiply ( stable cells e.g. muscle cells).

27
Q

What is atrophy

A

the decrease in the size of cells, tissue or organs leading to a reduction in the overall size or function. It affects fully developed organs or tissues but after a reason e.g. denervation or lack of activity e.g. immobilization after a fracture, the cell size is reduced leading to a shrinkage of the organ

28
Q

What is Aplasia

A

Aplasia is the complete or partial failure of an organ or tissue to develop during embryogenesis, resulting in its absence or underdevelopment e.g. fingers or appendices that don’t develop from birth

29
Q

Atrophy vs aplasia main difference

A

Atrophy involves a reduction in size of an already developed organ or tissue, while aplasia involves the absence or incomplete development of an organ or tissue from embryogenesis

30
Q

What is metaplasia

A

the change of a mature cell type into another mature cell type as an adaptive response to its environment. e.g. squamous metaplasia in the cervix (when columnar epithelial cells are replaced by stratified squamous epithelial cells) and bronchus and barrett’s metaplasia of the esophagus

31
Q

What is Dysplasia

A

a pre-malignant / disorganised growth of cells within a tissue characterised by a change in cell size and shape (pleomorphism), increased nuclear cytoplasmic ratio, increased mitotic activity and loss of organisation (all features of malignancy - if left untreated it can progress into a malignant form)

32
Q

What is an in-situ carcinoma

A

a localised tumour which has not yet invaded surrounding tissue. it is characterized by full-thickness dysplasia of epithelium, where abnormal cells are present but remain confined to the epithelium and have not invaded the basement membrane, preventing them from invading deeper tissues.

33
Q

what is an invasive carcinoma

A

In addition to full-thickness dysplasia of epithelium, the neoplastic cells have invaded beyond the original site, the stroma and invaded the basement membrane

34
Q

what are the two implications of invasive carcinomas

A
  1. you also have to take out the lymph nodes
  2. there is a worse prognosis in comparison to an in situ tumour.
35
Q

What is a carcinoma

A

a malignant tumour of epithelial differentiation

36
Q

what are further subdivisions of carcinomas

A
  • squamous cell carcinoma
  • Adenocarcinoma (derived from glandular epithelium)
  • Urothelial carcinoma (derived from urothelial cells)
    (these are based on the type of epithelial cell they derived from)
37
Q

What is a sarcoma

A

a malignant tumour of mesenchymal differentiation

38
Q

When defining a carcinoma and sarcoma why do you say of X “DIFFERENTIATION”

A

explains what you see under the microscope which you know for a fact and make your statement correct e.g. if there is an osteosarcoma in the breast which are still originally from epithelial origin but have differentiated ….

39
Q

what are further subdivisions of sarcomas

A
  • Fibrosarcoma (derived from fibrous connective tissue)
  • Leiomyosarcoma (derived from smooth muscle cells)
  • Rhabdomyosarcoma ( derived from skeletal muscle cells)
  • Liposarcoma ( derived from fat cells / adipocytes)
  • Chondrosarcoma (derived from cartilage cells)
  • Osteosarcoma ( derived from bone-forming cells / osteoblasts)
40
Q

What is a hamartoma

A

a developmental malformation (non-malignant). this will present as tissue which are normally present at the site but lay down differently which results in a lump e.g birh marks containing a lot of blood vessels or hair follicle

41
Q

what is a teratoma

A

a tumour of totipotent germ cells. this means that the cells can differentiate into various cell subtypes including bone, cartilage, muscle and epithelial cells which aren’t typically present in the organ e.g. teratoma in very or testis showing bone or cartilage

42
Q

hamartoma vs teratoma

A

a hamartoma is a benign growth of disorganised normal tissue in its usual location whilst teratomas are a neoplastic tumour (benign or malignant) that arise from germ cells and the cell type isn’t typical for the location

43
Q

Benign vs malignant tumous

A

Benign:
* smaller in size
* Well defined borders
* Low mitotic count
* Well differentiated
* localised to site of origin
* do not invade

Malignant:
* larger in size
* irregular borders
* high mitotic count
* variable differentiation
* spread to distant site (metastasis)
* invade into :
- basement membrane
- vascular channels
- perineual neural invasion
* have a worse prognosis

44
Q

Where can a benign tumour be fatal

A

in the brian (compresses structures)

45
Q

What is an adenoma

A

A benign tumour showing formation of glands

46
Q

what is a papilloma

A

a benign tumour showing formation of finger like / papillary structures

47
Q

adenoma vs papilloma

A

Adenomas are benign tumours originating from glandular tissue, while papillomas are benign epithelial tumours characterised by wart-like growths with finger-like projections.

48
Q

what is differentiation

A

the resemblance of tumour tissue to its normal cells of the tissue they originated from. beining and well differentiated malignant tumours show good resemblance e.g. fibroadenoma to normal lobules of breast (while poorly differentiated tumour cells look less like normal cells)

49
Q

what is anaplasia

A

refers to the loss of resemblance to its original tissue it originated from. this is a feature of malignancy. Anaplastic malignant tumours have bad prognosis (anaplastic cells usually lack the normal structure and function of the tissue they originated from being disorganised and pleomorphic)

50
Q

what is grading of tumous mean

A

how far the tumour is differentiated . this indicates how abnormal the cells are

51
Q

what does staging of tumors mean

A

how far the tumour is spread. this is a measure n terms of size of the primary tumour, the lumph node involvement and distant metastasis.

52
Q

what has UICC developed in order to stage tumours

A

TNM staging for various organ systems :
T- primary Tumour
N - Lymph Node
M - distant Metastasis

53
Q

T UICC ranks 1 - 4

A

T1 : 0-2cm
T2 : 2-5cm
T3 - more than 5cm
T4 - tumour has broken through the skin or attached to chest wall

54
Q

N UICC 0 - 3

A

N0 - Surgeon can’t fell any nodes
N1 - surgeon can feel swollen nodes
N2 - nodes feel swollen and lumpy
N3 - swollen nodes located near collarbone

55
Q

M UICC 0 - 1

A

M0 - tested nodes are cancer free
M1 - tested nodes show cancer cells are micrometastasis

56
Q

grading vs staging

A

Grading refers to the evaluation of how differentiated or abnormal cancer cells are, which helps determine the tumour’s aggressiveness and potential growth rate.
Staging refers to determining the extent of cancer within the body, including the size of the tumour, whether it has spread to nearby lymph nodes or other organs, and how advanced the cancer is. Staging helps guide treatment and assess prognosis